A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682783



Internal ID15072749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051238..4059672hg38UCSC Ensembl
Innerchr3:4092922..4101356hg19UCSC Ensembl
Innerchr3:4067922..4076356hg18UCSC Ensembl
Innerchr3:4067922..4076356hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg388435
hg198435
hg188435
hg178435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517232
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682783
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer